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m6A mRNA Destiny: Chained to the rhYTHm by the YTH-Containing Proteins
- Source :
- Genes, Vol 10, Iss 1, p 49 (2019), Genes, Genes, MDPI, 2019, 10 (1), pp.49. ⟨10.3390/genes10010049⟩
- Publication Year :
- 2019
- Publisher :
- MDPI AG, 2019.
-
Abstract
- International audience; The control of gene expression is a multi-layered process occurring at the level of DNA, RNA, and proteins. With the emergence of highly sensitive techniques, new aspects of RNA regulation have been uncovered leading to the emerging field of epitranscriptomics dealing with RNA modifications. Among those post-transcriptional modifications, N6-methyladenosine (m 6 A) is the most prevalent in messenger RNAs (mRNAs). This mark can either prevent or stimulate the formation of RNA-protein complexes, thereby influencing mRNA-related mechanisms and cellular processes. This review focuses on proteins containing a YTH domain (for YT521-B Homology), a small building block, that selectively detects the m 6 A nucleotide embedded within a consensus motif. Thereby, it contributes to the recruitment of various effectors involved in the control of mRNA fates through adjacent regions present in the different YTH-containing proteins.
- Subjects :
- m6A readers
0301 basic medicine
Adenosine
lcsh:QH426-470
YTH domain
[SDV.CAN]Life Sciences [q-bio]/Cancer
Nerve Tissue Proteins
[SDV.BC]Life Sciences [q-bio]/Cellular Biology
Review
Biology
Homology (biology)
mRNA methylation
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Epitranscriptomics
Gene expression
Genetics
Animals
Humans
RNA, Messenger
RNA Processing, Post-Transcriptional
Genetics (clinical)
Messenger RNA
Effector
RNA
[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology
[SDV.BIBS]Life Sciences [q-bio]/Quantitative Methods [q-bio.QM]
Cell biology
lcsh:Genetics
030104 developmental biology
chemistry
RNA Splicing Factors
MRNA methylation
epitranscriptomics
030217 neurology & neurosurgery
DNA
Subjects
Details
- ISSN :
- 20734425
- Volume :
- 10
- Database :
- OpenAIRE
- Journal :
- Genes
- Accession number :
- edsair.doi.dedup.....edfa219e0fa71f4c04a70f932c080fed
- Full Text :
- https://doi.org/10.3390/genes10010049